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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Bright light during the day doesn't change most human clock genes but may slightly increase Rev-erb-ß.

Targeting specific miRNAs may help treat hair follicle issues caused by hydrogen peroxide.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

FOXN1 duplication can cause excessive hair growth.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Urticadioica L extract may enhance human hair growth.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Certain genes are crucial for feather development in Wannan chickens.

A new gene variant causes curly coats in some dog breeds.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Protein ubiquitylation is crucial for controlling stem cell functions and could be targeted for cancer treatment.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Two new gene mutations cause a rare hair disorder.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Researchers found a non-functional sheep keratin gene due to mutations.

Monilethrix is linked to a gene cluster on chromosome 12.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.